반응 #54296
ord-87e20e5127b94517aacddcda20ba5ec1
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후처리
- 1workup.ADDITIONTo a suspension of 12.21 g
- 2workup.STIRRINGthe mixture stirred an additional 1/2 hour
- 3workup.ADDITIONTo the solution is added a solution of 9.88 g
- 4workup.STIRRINGAfter stirring for 24 hours
- 5기타the THF is removed in vacuo
- 6기타the residue partitioned with chloroform/water
- 7기타The oily residue is triturated with 300 ml
- 8기타benzene to give a white solid
- 9workup.DISSOLUTIONThis is dissolved in 50 ml
- 10온도cooled
- 11여과The white solid which forms is filtered
- 12기타air dried
실험 절차
To a suspension of 12.21 g. (0.05 moles) of methyl guanidine sulfate in 110 ml. of tetrahydrofuran is added 8.0 g. (0.10 moles of sodium hydroxide) of 50% aqueous sodium hydroxide. After stirring for 11/2 hours, 4.5 g. of sodium sulfate is slowly added and the mixture stirred an additional 1/2 hour. To the solution is added a solution of 9.88 g. (0.05 moles) of 2,6-dimethylphenyl-N-methylcarbamoyl chloride in 30 ml. of tetrahydrofuran. After stirring for 24 hours, the THF is removed in vacuo and the residue partitioned with chloroform/water. The oily residue is triturated with 300 ml. of hexane and 20 ml. benzene to give a white solid. This is dissolved in 50 ml. of 1:4 HNO3 and warmed slightly over 1/2 hour, then cooled. The white solid which forms is filtered and air dried to obtain 1-(2',6'-dimethylphenyl)-1-methyl-3-methylamidinourea nitrate.